Canonical Allele Identifier: CA2610725962
Gene: CYP17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837525A>G , CM000672.2:g.102837525A>G GRCh38
NC_000010.10:g.104597282A>G , CM000672.1:g.104597282A>G GRCh37
NC_000010.9:g.104587272A>G NCBI36
NG_007955.1:g.5009T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.3:c.-164T>C ENSP00000358903.3:n.-164T>C
NM_000102.3:c.-164T>C NP_000093.1:n.-164T>C